3.5 Flashcards
The polymerase chain reaction (PCR) is an…
artificial method of replicating DNA under laboratory conditions
The PCR technique is used to…
amplify large quantities of a specific sequence of DNA from an initial minute sample
Each reaction cycle…
doubles the amount of DNA – a standard PCR sequence of 30 cycles creates over 1 billion copies (230)
Stages of PCR
PCR occurs in a thermal cycler and uses variations in temperature to control the replication process via three steps:
PCR Denaturation
DNA sample is heated to separate it into two single strands (~95ºC for 1 min)
PCR Annealing
DNA primers attach to the 3’ ends of the target sequence (~55ºC for 1 min)
PCR Elongation
A heat-tolerant DNA polymerase (Taq) binds to the primer and copies the strand (~72ºC for 2 min)
Gel electrophoresis is a laboratory technique used to…
separate and isolate proteins or DNA fragments based on mass / size
Gel electrophoresis process
- Samples are placed in a block of gel and an electric current is applied which causes the samples to move through the gel
- Smaller samples are less impeded by the gel matrix and hence will move faster through the gel
- This causes samples of different sizes to separate as they travel at different speeds
Gel electrophoresis: DNA separation
- DNA may be cut into fragments using restriction endonuclease – different DNA samples will generate different fragment lengths
- Fragments separate because DNA is negatively charged due to the presence of a phosphate group (PO43–) on each nucleotide
- DNA samples are placed into an agarose gel and fragment size calculated by comparing against known industry standards
- Specific sequences can be identified by incorporating a complementary radiolabelled hybridisation probe, transferring the separated sequences to a membrane and then visualising via autoradiography (Southern blotting)
Gel electrophoresis: Protein separation
- Proteins may be folded into a variety of shapes (affecting size) and have positive and negative regions (no clear charge)
- Proteins must first be treated with an anionic detergent (SDS) in order to linearise and impart a uniform negative charge
- Protein samples are placed into a polyacrylamide gel and sizes compared against known industry standards
- Separated proteins are transferred to a membrane and then target proteins are identified by staining with specific monoclonal antibodies (Western blotting)
DNA profiling is a technique by which…
individuals can be identified and compared via their respective DNA profiles
Within the non-coding regions of an individual’s genome there exists…
satellite DNA – long stretches of DNA made up of repeating elements called short tandem repeats (STRs)
- As individuals will likely have different numbers of repeats at a given satellite DNA locus, they will generate unique DNA profiles
DNA profiling is commonly used in…
criminal investigations (forensics) and to settle paternity disputes
The DNA profiling procedure involved is common for both:
- A DNA sample is collected (e.g. from blood, semen, saliva, etc.) and then amplified using PCR
- Satellite DNA (with STR sequences) are cut with specific restriction enzymes to generate fragments
- Fragment length will differ between individuals due to the variable length of their short tandem repeats
- The fragments are separated using gel electrophoresis and the resulting profiles are compared
Forensic Investigations:
Suspects should be a complete match with the DNA sample taken from the crime scene if a conviction is to occur
The number of loci used to generate a unique profile depends on the size of the population being compared
- E.g. America (population: ~ 320 million) uses 13 loci for comparison; Australia (population: ~ 25 million) uses only 9 loci
Paternity Testing:
Children inherit half their chromosomes from each parent and thus should possess a combination of parental fragments
In other words, all fragments produced in the child should also be produced by either the mother or father
A gene determines a…
particular trait by encoding for a specific polypeptide in a given organism
- Because the genetic code is (almost) universal, an organism can potentially express a new trait if the appropriate gene is introduced into its genome
transgenic
The transfer of genes between species is called gene modification, and the new organism created is called a transgenic
The process of gene transfer can be summarised in four key steps:
- Isolation of gene and vector (by PCR)
- Digestion of gene and vector (by restriction endonuclease)
- Ligation of gene and vector (by DNA ligase)
- Selection and expression of transgenic construct